Novel genes/loci validate the small effect size of ERBB2 in patients with myasthenia gravis
Author:
Affiliation:
1. College of Bioinformatics Science and Technology, Harbin Medical University, Harbin 150081, China
2. NHC and CAMS Key Laboratory of Molecular Probe and Targeted Theranostics, Harbin Medical University, Harbin 150028, China
Funder
National Natural Science Foundation of China
Tou-Yan Innovation Team Program of Heilongjiang Province
Publisher
Proceedings of the National Academy of Sciences
Subject
Multidisciplinary
Link
https://pnas.org/doi/pdf/10.1073/pnas.2207273119
Reference10 articles.
1. Identification of genetic risk loci and prioritization of genes and pathways for myasthenia gravis: a genome-wide association study
2. Mendelian randomization: genetic anchors for causal inference in epidemiological studies
3. Mendelian Randomization
4. Genetic mechanisms of critical illness in COVID-19
5. Type 2 Diabetes as a Determinant of Parkinson's Disease Risk and Progression
Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Reply to Zhu et al.: Implications ofCHRNB1andERBB2in the pathobiology of myasthenia gravis;Proceedings of the National Academy of Sciences;2022-08-15
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